Characterization of an extracellular dipeptidase from Streptococcus gordonii FSS2

Infect Immun. 2005 Feb;73(2):1256-9. doi: 10.1128/IAI.73.2.1256-1259.2005.

Abstract

PepV, a dipeptidase found in culture fluids of Streptococcus gordonii FSS2, was purified and characterized, and its gene was cloned. PepV is a monomeric metalloenzyme of approximately 55 kDa that preferentially degrades hydrophobic dipeptides. The gene encodes a polypeptide of 467 amino acids, with a theoretical molecular mass of 51,114 Da and a calculated pI of 4.8. The S. gordonii PepV gene is homologous to the PepV gene family from Lactobacillus and Lactococcus spp.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Dipeptidases / genetics
  • Dipeptidases / isolation & purification
  • Dipeptidases / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Molecular Sequence Data
  • Streptococcus / enzymology*
  • Streptococcus / genetics
  • Streptococcus / metabolism
  • Substrate Specificity

Substances

  • Dipeptidases

Associated data

  • GENBANK/AY496433